戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 869618作成日:2026年10月26日

Ammonium Chloride → 2-(8-bromo-3-fluorodibenzo[b,e]oxepin-11(6H)-ylidene)propanenitrile

https://huagongshe.com/reaction/869618

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Diethyl (1-cyanoethyl)phosphonateHCID 282103—
反応物Lithium diisopropylamideHCID 2724682—
反応物8-Bromo-3-fluorodibenzo[b,e]oxepin-11(6H)-oneHCID 86721485—
溶媒TetrahydrofuranHCID 8028—
生成物2-(8-bromo-3-fluorodibenzo[b,e]oxepin-11(6H)-ylidene)propanenitrileHCID 8672148492.2%

反応条件

温度0 °C

反応手順

[step 3] Commercially available diethyl 1-cyanoethylphosphonate (38.0 g, 199 mmol) was dissolved in THF (170 mL), LDA (99.0 mL, 199 mmol, 2.0 mol/L heptane/THF/ethylbenzene solution) was added dropwise at 0° C., and the mixture was stirred at 0° C. for 1 hr. 8-Bromo-3-fluorodibenzo[b,e]oxepin-11(6H)-one (30.5 g, 99.0 mmol) obtained in step 2 and dissolved in THF (120 ml) was added to the reaction system, and the mixture was stirred at room temperature for 1 hr. To the mixture was added saturated aqueous ammonium chloride solution (500 mL), and the mixture was extracted 3 times with ethyl acetate. The combined organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/0 v/v-80/20 v/v) to give 2-(8-bromo-3-fluorodibenzo[b,e]oxepin-11(6H)-ylidene)propanenitrile (31.4 g, 92%, E/Z=1/1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08969345B2
出典データセットuspto-grants-2015_03
ORD IDord-8254010677a94a17a19b9a6951006130
出典メモuspto-grants-2015_03